Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP258497.RA25m7GvnTWkYYCUQ1oPl2zNyaRYgQLDvZePyvT-bhKfA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP258497.RA25m7GvnTWkYYCUQ1oPl2zNyaRYgQLDvZePyvT-bhKfA130_assertion type Assertion NP258497.RA25m7GvnTWkYYCUQ1oPl2zNyaRYgQLDvZePyvT-bhKfA130_head.
- NP258497.RA25m7GvnTWkYYCUQ1oPl2zNyaRYgQLDvZePyvT-bhKfA130_assertion description "[PRRT2 mutations are associated with a wide range of clinical syndromes: the various paroxysmal dyskinesias, infantile seizures, paroxysmal torticollis, migraine, hemiplegic migraine, episodic ataxia and even intellectual disability in the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258497.RA25m7GvnTWkYYCUQ1oPl2zNyaRYgQLDvZePyvT-bhKfA130_provenance.
- NP258497.RA25m7GvnTWkYYCUQ1oPl2zNyaRYgQLDvZePyvT-bhKfA130_assertion evidence source_evidence_literature NP258497.RA25m7GvnTWkYYCUQ1oPl2zNyaRYgQLDvZePyvT-bhKfA130_provenance.
- NP258497.RA25m7GvnTWkYYCUQ1oPl2zNyaRYgQLDvZePyvT-bhKfA130_assertion SIO_000772 23398397 NP258497.RA25m7GvnTWkYYCUQ1oPl2zNyaRYgQLDvZePyvT-bhKfA130_provenance.
- NP258497.RA25m7GvnTWkYYCUQ1oPl2zNyaRYgQLDvZePyvT-bhKfA130_assertion wasDerivedFrom befree-20140225 NP258497.RA25m7GvnTWkYYCUQ1oPl2zNyaRYgQLDvZePyvT-bhKfA130_provenance.
- NP258497.RA25m7GvnTWkYYCUQ1oPl2zNyaRYgQLDvZePyvT-bhKfA130_assertion wasGeneratedBy ECO_0000203 NP258497.RA25m7GvnTWkYYCUQ1oPl2zNyaRYgQLDvZePyvT-bhKfA130_provenance.